Home |
Help |
Advanced search
2025-05-09 16:52:09, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_005445 4131 bp mRNA linear PRI 26-MAY-2013
DEFINITION Homo sapiens structural maintenance of chromosomes 3 (SMC3), mRNA.
ACCESSION NM_005445
VERSION NM_005445.3 GI:63054826
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 4131)
AUTHORS Gimigliano,A., Mannini,L., Bianchi,L., Puglia,M., Deardorff,M.A.,
Menga,S., Krantz,I.D., Musio,A. and Bini,L.
TITLE Proteomic profile identifies dysregulated pathways in Cornelia de
Lange syndrome cells with distinct mutations in SMC1A and SMC3
genes
JOURNAL J. Proteome Res. 11 (12), 6111-6123 (2012)
PUBMED 23106691
REMARK GeneRIF: c-MYC down-regulation caused by cohesin mutations in SMC1A
and SMC3 genes may be an early/primary event in the pathogenesis of
Cornelia de Lange syndrome.
REFERENCE 2 (bases 1 to 4131)
AUTHORS Chatfield,K.C., Schrier,S.A., Li,J., Clark,D., Kaur,M., Kline,A.D.,
Deardorff,M.A., Jackson,L.S., Goldmuntz,E. and Krantz,I.D.
TITLE Congenital heart disease in Cornelia de Lange syndrome: phenotype
and genotype analysis
JOURNAL Am. J. Med. Genet. A 158A (10), 2499-2505 (2012)
PUBMED 22965847
REMARK GeneRIF: NIPBL, SMC1A, and SMC3 mutation-positive patients were
equally likely to have congenital heart diseases in Cornelia de
lange syndrome.
REFERENCE 3 (bases 1 to 4131)
AUTHORS Li,Z.T., Wang,W., Zhao,Y., Wang,L.X., Zhu,H.S., Wu,W.D. and Wu,Y.M.
TITLE [Change of structural maintenance of chromosome (SMC)1, SMC3,
Separase and Securin expression in BEAS-2B malignant transformation
cell induced by coal tar pitch smoke extracts]
JOURNAL Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi 28 (10), 776-780
(2010)
PUBMED 21126432
REMARK GeneRIF: SMC3 and separase are upregulated and securin is
downregulated in malignant transformation of BEAS-2B cells induced
by coal tar pitch smoke extracts.
REFERENCE 4 (bases 1 to 4131)
AUTHORS Pie,J., Gil-Rodriguez,M.C., Ciero,M., Lopez-Vinas,E., Ribate,M.P.,
Arnedo,M., Deardorff,M.A., Puisac,B., Legarreta,J., de Karam,J.C.,
Rubio,E., Bueno,I., Baldellou,A., Calvo,M.T., Casals,N.,
Olivares,J.L., Losada,A., Hegardt,F.G., Krantz,I.D.,
Gomez-Puertas,P. and Ramos,F.J.
TITLE Mutations and variants in the cohesion factor genes NIPBL, SMC1A,
and SMC3 in a cohort of 30 unrelated patients with Cornelia de
Lange syndrome
JOURNAL Am. J. Med. Genet. A 152A (4), 924-929 (2010)
PUBMED 20358602
REMARK GeneRIF: The identification of 14 additional mutations of the
cohesin complex genes NIPBL and SMC1A in a cohort of 30 unrelated
patients with Cornelia de Lange syndrome, is reported.
GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 5 (bases 1 to 4131)
AUTHORS Terret,M.E., Sherwood,R., Rahman,S., Qin,J. and Jallepalli,P.V.
TITLE Cohesin acetylation speeds the replication fork
JOURNAL Nature 462 (7270), 231-234 (2009)
PUBMED 19907496
REFERENCE 6 (bases 1 to 4131)
AUTHORS Sumara,I., Vorlaufer,E., Gieffers,C., Peters,B.H. and Peters,J.M.
TITLE Characterization of vertebrate cohesin complexes and their
regulation in prophase
JOURNAL J. Cell Biol. 151 (4), 749-762 (2000)
PUBMED 11076961
REFERENCE 7 (bases 1 to 4131)
AUTHORS Ghiselli,G. and Iozzo,R.V.
TITLE Overexpression of bamacan/SMC3 causes transformation
JOURNAL J. Biol. Chem. 275 (27), 20235-20238 (2000)
PUBMED 10801778
REFERENCE 8 (bases 1 to 4131)
AUTHORS Schmiesing,J.A., Ball,A.R. Jr., Gregson,H.C., Alderton,J.M.,
Zhou,S. and Yokomori,K.
TITLE Identification of two distinct human SMC protein complexes involved
in mitotic chromosome dynamics
JOURNAL Proc. Natl. Acad. Sci. U.S.A. 95 (22), 12906-12911 (1998)
PUBMED 9789013
REFERENCE 9 (bases 1 to 4131)
AUTHORS Shimizu,K., Shirataki,H., Honda,T., Minami,S. and Takai,Y.
TITLE Complex formation of SMAP/KAP3, a KIF3A/B ATPase motor-associated
protein, with a human chromosome-associated polypeptide
JOURNAL J. Biol. Chem. 273 (12), 6591-6594 (1998)
PUBMED 9506951
REFERENCE 10 (bases 1 to 4131)
AUTHORS Gupta,K., Anand,G., Yin,X., Grove,L. and Prochownik,E.V.
TITLE Mmip1: a novel leucine zipper protein that reverses the suppressive
effects of Mad family members on c-myc
JOURNAL Oncogene 16 (9), 1149-1159 (1998)
PUBMED 9528857
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from CA439554.1, AF020043.1 and
AL359260.20.
This sequence is a reference standard in the RefSeqGene project.
On May 5, 2005 this sequence version replaced gi:24475891.
Summary: This gene belongs to the SMC3 subfamily of SMC proteins.
The encoded protein occurs in certain cell types as either an
intracellular, nuclear protein or a secreted protein. The nuclear
form, known as structural maintenance of chromosomes 3, is a
component of the multimeric cohesin complex that holds together
sister chromatids during mitosis, enabling proper chromosome
segregation. Post-translational modification of the encoded protein
by the addition of chondroitin sulfate chains gives rise to the
secreted proteoglycan bamacan, an abundant basement membrane
protein. [provided by RefSeq, Jul 2008].
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: AF020043.1, AK289771.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025081, ERS025082 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-74 CA439554.1 15-88
75-3164 AF020043.1 40-3129
3165-3165 AL359260.20 78758-78758
3166-4131 AF020043.1 3131-4096
FEATURES Location/Qualifiers
source 1..4131
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="10"
/map="10q25"
gene 1..4131
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/note="structural maintenance of chromosomes 3"
/db_xref="GeneID:9126"
/db_xref="HGNC:2468"
/db_xref="HPRD:05829"
/db_xref="MIM:606062"
exon 1..141
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 28
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="c"
/db_xref="dbSNP:148267784"
misc_feature 49..51
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/note="upstream in-frame stop codon"
variation 53
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="c"
/db_xref="dbSNP:376252081"
variation 65
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:183537656"
variation 66
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="g"
/db_xref="dbSNP:370204751"
variation 92
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="g"
/replace="t"
/db_xref="dbSNP:374449319"
CDS 127..3780
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/note="chondroitin sulfate proteoglycan 6 (bamacan);
basement membrane-associated chondroitin proteoglycan;
chromosome-associated polypeptide; SMC-3; SMC protein 3"
/codon_start=1
/product="structural maintenance of chromosomes protein 3"
/protein_id="NP_005436.1"
/db_xref="GI:4885399"
/db_xref="CCDS:CCDS31285.1"
/db_xref="GeneID:9126"
/db_xref="HGNC:2468"
/db_xref="HPRD:05829"
/db_xref="MIM:606062"
/translation="
MYIKQVIIQGFRSYRDQTIVDPFSSKHNVIVGRNGSGKSNFFYAIQFVLSDEFSHLRPEQRLALLHEGTGPRVISAFVEIIFDNSDNRLPIDKEEVSLRRVIGAKKDQYFLDKKMVTKNDVMNLLESAGFSRSNPYYIVKQGKINQMATAPDSQRLKLLREVAGTRVYDERKEESISLMKETEGKREKINELLKYIEERLHTLEEEKEELAQYQKWDKMRRALEYTIYNQELNETRAKLDELSAKRETSGEKSRQLRDAQQDARDKMEDIERQVRELKTKISAMKEEKEQLSAERQEQIKQRTKLELKAKDLQDELAGNSEQRKRLLKERQKLLEKIEEKQKELAETEPKFNSVKEKEERGIARLAQATQERTDLYAKQGRGSQFTSKEERDKWIKKELKSLDQAINDKKRQIAAIHKDLEDTEANKEKNLEQYNKLDQDLNEVKARVEELDRKYYEVKNKKDELQSERNYLWREENAEQQALAAKREDLEKKQQLLRAATGKAILNGIDSINKVLDHFRRKGINQHVQNGYHGIVMNNFECEPAFYTCVEVTAGNRLFYHIVDSDEVSTKILMEFNKMNLPGEVTFLPLNKLDVRDTAYPETNDAIPMISKLRYNPRFDKAFKHVFGKTLICRSMEVSTQLARAFTMDCITLEGDQVSHRGALTGGYYDTRKSRLELQKDVRKAEEELGELEAKLNENLRRNIERINNEIDQLMNQMQQIETQQRKFKASRDSILSEMKMLKEKRQQSEKTFMPKQRSLQSLEASLHAMESTRESLKAELGTDLLSQLSLEDQKRVDALNDEIRQLQQENRQLLNERIKLEGIITRVETYLNENLRKRLDQVEQELNELRETEGGTVLTATTSELEAINKRVKDTMARSEDLDNSIDKTEAGIKELQKSMERWKNMEKEHMDAINHDTKELEKMTNRQGMLLKKKEECMKKIRELGSLPQEAFEKYQTLSLKQLFRKLEQCNTELKKYSHVNKKALDQFVNFSEQKEKLIKRQEELDRGYKSIMELMNVLELRKYEAIQLTFKQVSKNFSEVFQKLVPGGKATLVMKKGDVEGSQSQDEGEGSGESERGSGSQSSVPSVDQFTGVGIRVSFTGKQGEMREMQQLSGGQKSLVALALIFAIQKCDPAPFYLFDEIDQALDAQHRKAVSDMIMELAVHAQFITTTFRPELLESADKFYGVKFRNKVSHIDVITAEMAKDFVEDDTTHG
"
misc_feature 127..3708
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/note="Chromosome segregation ATPases [Cell division and
chromosome partitioning]; Region: Smc; COG1196"
/db_xref="CDD:224117"
misc_feature 133..>600
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/note="ATP-binding cassette domain of eukaryotic SMC3
proteins; Region: ABC_SMC3_euk; cd03272"
/db_xref="CDD:213239"
misc_feature 220..243
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/note="Walker A/P-loop; other site"
/db_xref="CDD:213239"
misc_feature order(229..234,238..246,547..549)
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/note="ATP binding site [chemical binding]; other site"
/db_xref="CDD:213239"
misc_feature 439..441
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/experiment="experimental evidence, no additional details
recorded"
/note="N6-acetyllysine; propagated from
UniProtKB/Swiss-Prot (Q9UQE7.2); acetylation site"
misc_feature 442..444
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/experiment="experimental evidence, no additional details
recorded"
/note="N6-acetyllysine; propagated from
UniProtKB/Swiss-Prot (Q9UQE7.2); acetylation site"
misc_feature 538..549
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/note="Q-loop/lid; other site"
/db_xref="CDD:213239"
misc_feature 544..546
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/experiment="experimental evidence, no additional details
recorded"
/note="N6-acetyllysine; propagated from
UniProtKB/Swiss-Prot (Q9UQE7.2); acetylation site"
misc_feature <1288..>1572
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/note="The Bin/Amphiphysin/Rvs (BAR) domain, a
dimerization module that binds membranes and detects
membrane curvature; Region: BAR; cl12013"
/db_xref="CDD:245835"
misc_feature 1639..2127
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (Q9UQE7.2);
Region: Flexible hinge"
misc_feature 1714..2052
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/note="SMC proteins Flexible Hinge Domain; Region:
SMC_hinge; smart00968"
/db_xref="CDD:214944"
misc_feature 2473..2475
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphothreonine; propagated from
UniProtKB/Swiss-Prot (Q9UQE7.2); phosphorylation site"
misc_feature 2485..2487
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q9UQE7.2); phosphorylation site"
misc_feature 2485..2487
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 3319..3321
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q9UQE7.2); phosphorylation site"
misc_feature 3319..3321
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 3325..3327
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q9UQE7.2); phosphorylation site"
misc_feature 3325..3327
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 3346..3348
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 3373..3375
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q9UQE7.2); phosphorylation site"
misc_feature 3373..3375
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature <3439..3723
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/note="ATP-binding cassette transporter nucleotide-binding
domain; Region: ABC_ATPase; cl17201"
/db_xref="CDD:247755"
misc_feature 3469..3498
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/note="ABC transporter signature motif; other site"
/db_xref="CDD:213179"
misc_feature 3541..3558
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/note="Walker B; other site"
/db_xref="CDD:213179"
misc_feature 3565..3576
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/note="D-loop; other site"
/db_xref="CDD:213179"
misc_feature 3637..3657
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/note="H-loop/switch region; other site"
/db_xref="CDD:213179"
misc_feature 3694..3696
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/experiment="experimental evidence, no additional details
recorded"
/note="N6-acetyllysine; propagated from
UniProtKB/Swiss-Prot (Q9UQE7.2); acetylation site"
exon 142..217
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
exon 218..256
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 238
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:79203236"
exon 257..324
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
exon 325..396
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 381
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:146433240"
exon 397..476
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 402
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:199936534"
variation 468
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:139894626"
exon 477..555
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 503
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:113411202"
variation 510
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376176857"
variation 535
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:370788296"
exon 556..673
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
STS 602..720
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/standard_name="SMC3-1"
/db_xref="UniSTS:513658"
variation 633
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:370909218"
exon 674..849
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 750
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="c"
/db_xref="dbSNP:367803262"
variation 840
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:144306349"
variation 846
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:144281914"
exon 850..930
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
exon 931..1095
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 936
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:148729748"
variation 942
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:142262783"
variation 963
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:151335692"
exon 1096..1217
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 1119
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="g"
/db_xref="dbSNP:369244486"
variation 1158
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="g"
/db_xref="dbSNP:140210218"
variation 1175
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:145610953"
exon 1218..1431
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 1244
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:377731006"
variation 1296
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="c"
/db_xref="dbSNP:147721344"
variation 1320
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:141561837"
variation 1406
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:142524280"
exon 1432..1535
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 1440
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369744445"
variation 1458
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="g"
/db_xref="dbSNP:150125754"
variation 1491
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:75323904"
variation 1510
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:370302318"
exon 1536..1635
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 1631..1632
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace=""
/replace="g"
/db_xref="dbSNP:34449308"
exon 1636..1796
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 1663
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:377039037"
variation 1664
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:190230933"
variation 1700
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:148832992"
variation 1707
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:182445355"
variation 1719
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="g"
/db_xref="dbSNP:374832653"
variation 1725
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="g"
/replace="t"
/db_xref="dbSNP:200551010"
exon 1797..1938
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 1806
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:75817442"
exon 1939..2089
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 2001
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:137867426"
variation 2016
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="t"
/db_xref="dbSNP:79046607"
exon 2090..2242
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 2124
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="g"
/db_xref="dbSNP:142669130"
variation 2133
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:147404470"
variation 2188
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="g"
/db_xref="dbSNP:201162818"
variation 2194
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:377463176"
variation 2228
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:371216768"
exon 2243..2394
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 2295
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="g"
/db_xref="dbSNP:138714964"
variation 2296
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="g"
/db_xref="dbSNP:141257272"
variation 2335
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:376690548"
variation 2344
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="c"
/db_xref="dbSNP:371259753"
variation 2352
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:150649173"
variation 2357
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:74515128"
variation 2382
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="g"
/db_xref="dbSNP:199634096"
variation 2390
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:76568464"
exon 2395..2553
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 2425
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139763232"
variation 2455
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:76625999"
exon 2554..2661
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 2619
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:112525060"
exon 2662..2770
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
exon 2771..3018
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 2781
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:369169661"
variation 2820..2821
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace=""
/replace="c"
/db_xref="dbSNP:36066882"
variation 2836
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:112281749"
variation 2908
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="c"
/db_xref="dbSNP:202034783"
variation 2922
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199966664"
variation 2956
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:139627416"
exon 3019..3231
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 3060
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147463420"
variation 3090
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:111611128"
variation 3108
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="g"
/db_xref="dbSNP:201308737"
variation 3165
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:2419565"
exon 3232..3423
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 3240
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368894572"
variation 3247
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:372599261"
variation 3261
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:373337157"
variation 3384
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:145702274"
variation 3385
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:147743879"
variation 3390
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="c"
/db_xref="dbSNP:377499428"
exon 3424..3601
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 3447
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:184870066"
variation 3465
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:189703529"
variation 3504
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:140946653"
variation 3534
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:374061811"
exon 3602..3708
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 3610
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:368832369"
variation 3621
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="t"
/db_xref="dbSNP:142395521"
variation 3624
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:201318099"
exon 3709..4112
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/inference="alignment:Splign:1.39.8"
variation 3734
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368353204"
variation 3791
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:371970542"
variation 3797
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:199611616"
variation 3811
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:200928191"
variation 3817
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:191584262"
variation 3830
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="g"
/db_xref="dbSNP:368890227"
variation 3935
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:368999586"
variation 3938
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:183542538"
variation 4077
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="t"
/db_xref="dbSNP:188322637"
polyA_signal 4088..4093
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
variation 4099
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:190225025"
variation 4109
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="c"
/replace="t"
/db_xref="dbSNP:182524436"
polyA_site 4112
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
variation 4112
/gene="SMC3"
/gene_synonym="BAM; BMH; CDLS3; CSPG6; HCAP; SMC3L1"
/replace="a"
/replace="g"
/db_xref="dbSNP:117538515"
ORIGIN
ttttgtttggctgaggggagcgagcggcgctttgggggaggggtcgcgtaggcgcctcacctgaccctgcggccgtgcggttgctgctccggggcaggtctccttccaggccaggggcccggaatcatgtacataaagcaggtgattatccagggttttcgaagttacagagatcaaacaattgtagatcccttcagttcaaaacataatgtgattgtgggcagaaatggatctggaaaaagtaactttttttatgcaattcagtttgttctcagtgatgagtttagtcatcttcgtccagaacagcggttggctttattgcatgaaggtactggtcctcgtgttatttctgcttttgtggagattatttttgataattcagacaaccggttaccaatcgataaagaggaagtttcacttcgaagagttattggtgccaaaaaggatcagtatttcttagacaagaagatggtcacgaaaaatgatgtgatgaacctccttgaaagcgctggtttttctcgaagcaatccttattatattgttaaacaaggaaagatcaaccagatggcaacagcaccagattctcagagattaaagctattaagagaagtagctggtactagagtgtatgacgaacgaaaggaagaaagcatctccttaatgaaagaaacagagggcaaacgggaaaaaatcaatgagttgttaaaatacattgaagagagattacatactctagaggaagaaaaggaagaactagctcagtatcagaagtgggataaaatgagacgagccctggaatataccatttacaatcaggaacttaacgagactcgtgccaaacttgatgagctttctgctaagcgagagactagtggagaaaaatccagacaattaagagatgctcagcaggatgcaagagataaaatggaggatatcgaacgccaagttagagaattgaaaacaaaaatttcagctatgaaagaagaaaaagaacagcttagtgctgaaagacaagagcagattaagcagaggactaagttggagcttaaagccaaggatttacaagatgaactagcaggcaatagtgaacaaaggaaacgtttattaaaagagaggcagaagctgcttgaaaaaatagaagaaaagcagaaagaactggcagaaacagaacccaaattcaacagtgtgaaagagaaagaagaacgaggaattgctagattggctcaagctacccaggaaagaacggatctttatgcaaagcagggtcgaggaagccagtttacatcaaaagaagaaagggataagtggattaaaaaggaactcaagtctttagatcaggctattaatgacaagaaaagacagattgctgctatacataaggatttggaagacactgaagcaaataaagagaaaaatctggagcagtataataaactggaccaggatcttaatgaagtcaaagctcgagtagaagaactggacagaaaatattacgaagtaaaaaataagaaagatgaactacaaagtgaaagaaactacttgtggagagaagagaatgcagaacagcaagcacttgctgctaaaagagaagatcttgaaaagaagcaacaacttcttagagcagcaacaggaaaggccattttaaatggaatagacagcataaacaaagtgctagaccacttccgtcgaaaaggaataaaccagcatgttcaaaatggctatcatggtattgtaatgaataactttgaatgtgaaccagctttctacacatgcgtggaagtcactgctggaaacaggttattttatcacattgttgattcagatgaagtcagcacgaagattttaatggagtttaataaaatgaatcttcctggagaggttacttttctgcctcttaacaagttagatgtcagggatacagcctatcctgaaaccaatgatgctattcctatgatcagcaaactgaggtacaatcccagatttgacaaagctttcaaacatgtgtttggaaagactcttatttgtcgtagcatggaagtttcaacccagctggcccgtgctttcactatggactgtattactttggaaggtgaccaagtcagccatcggggtgctctaactgggggttattatgacacaaggaagtctcgacttgaattgcaaaaagatgttagaaaagcagaagaagaactaggtgaacttgaagcaaagctcaatgaaaacctgcgcagaaatattgaaaggattaataatgaaattgatcagttgatgaaccaaatgcaacagatcgagacccagcaaaggaaatttaaagcatctagagatagcatattatcagaaatgaagatgctaaaagagaagaggcagcagtcagagaaaaccttcatgcctaagcaacgtagcttacagagtttggaggcaagcttgcatgctatggagtctaccagagagtcattgaaagcagaactgggaactgatttgctttctcaactgagtttggaagatcagaagagagtagatgcactgaatgatgagattcgtcaacttcagcaggaaaacagacagttgctaaatgaaagaattaaattagaaggtattattactcgagtagagacttatctcaatgagaatctgagaaaacgcttggaccaagtagaacaggaacttaatgagctgagagagacagaagggggtactgttctcacagccacaacatcagaacttgaagccatcaataaaagagtaaaagacactatggcacgatcagaagatttggacaattccattgataaaacagaagctggaattaaggagcttcagaagagtatggagcgctggaaaaatatggaaaaagaacatatggatgctataaatcatgatactaaagaactggaaaagatgacaaatcggcaaggcatgctattgaagaagaaagaagagtgtatgaagaaaattcgagaacttggatcacttccccaggaagcatttgaaaagtaccagacactgagcctcaaacagttgtttcgaaaacttgagcagtgcaacacagaattaaagaagtacagccatgttaacaaaaaggctttggatcagtttgtaaatttctccgagcagaaagaaaagttaataaagcgtcaagaagagttagataggggttacaaatcaatcatggaactgatgaatgtacttgaacttcggaaatatgaagctattcagttaactttcaaacaggtatctaagaacttcagtgaagtattccagaagttagtacctggtggcaaagctactttggtgatgaagaaaggagatgtggagggcagtcagtctcaagatgaaggagaagggagtggtgagagtgagaggggttctggctcacaaagcagtgtcccatcagttgaccagtttactggagttggaattagggtgtcatttacaggaaaacaaggtgaaatgagagaaatgcaacagctttcaggtggacagaaatccttggtagcccttgctctgatttttgccattcagaaatgtgacccggctccattttacttgtttgatgaaattgaccaggctctggatgctcagcacagaaaggctgtgtcagatatgattatggaacttgctgtacatgctcagtttattacaactacttttaggcctgaactgcttgagtcagctgacaaattctatggtgtaaagttcagaaataaggttagtcatattgatgtgatcacagcagagatggccaaagactttgtagaagatgataccacacatggttaattggaaaatactacctactggtttgggagatgtatatagtaatatgattctcatacccaggaactgtaaatttaaacctaaatatttggccaatagttttcagacttaaagcatcatagtccttttatatttgtctttgtattttataagatactctgtaatgtcatgtttgtactgatagtttaagaatttaatttcctgtacaactttttgtaaaatgttctgctcctattttaaatgttttgaaacatgctaaatattctttcctaattattttatcacttatactaccttttttatagcttcaattaaataatcggttttatgactaaaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:9126 -> Molecular function: GO:0003682 [chromatin binding] evidence: IEA
GeneID:9126 -> Molecular function: GO:0003777 [microtubule motor activity] evidence: NAS
GeneID:9126 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:9126 -> Molecular function: GO:0005524 [ATP binding] evidence: IEA
GeneID:9126 -> Molecular function: GO:0036033 [mediator complex binding] evidence: IEA
GeneID:9126 -> Molecular function: GO:0045502 [dynein binding] evidence: IDA
GeneID:9126 -> Molecular function: GO:0046982 [protein heterodimerization activity] evidence: IPI
GeneID:9126 -> Biological process: GO:0000278 [mitotic cell cycle] evidence: TAS
GeneID:9126 -> Biological process: GO:0000910 [cytokinesis] evidence: TAS
GeneID:9126 -> Biological process: GO:0006275 [regulation of DNA replication] evidence: IMP
GeneID:9126 -> Biological process: GO:0006281 [DNA repair] evidence: IEA
GeneID:9126 -> Biological process: GO:0007052 [mitotic spindle organization] evidence: IEP
GeneID:9126 -> Biological process: GO:0007062 [sister chromatid cohesion] evidence: IMP
GeneID:9126 -> Biological process: GO:0007062 [sister chromatid cohesion] evidence: NAS
GeneID:9126 -> Biological process: GO:0007067 [mitosis] evidence: IEA
GeneID:9126 -> Biological process: GO:0007126 [meiosis] evidence: IDA
GeneID:9126 -> Biological process: GO:0007165 [signal transduction] evidence: IDA
GeneID:9126 -> Biological process: GO:0019827 [stem cell maintenance] evidence: IEA
GeneID:9126 -> Biological process: GO:0032876 [negative regulation of DNA endoreduplication] evidence: IMP
GeneID:9126 -> Cellular component: GO:0000775 [chromosome, centromeric region] evidence: TAS
GeneID:9126 -> Cellular component: GO:0000785 [chromatin] evidence: IDA
GeneID:9126 -> Cellular component: GO:0000800 [lateral element] evidence: IEA
GeneID:9126 -> Cellular component: GO:0000922 [spindle pole] evidence: IDA
GeneID:9126 -> Cellular component: GO:0005604 [basement membrane] evidence: TAS
GeneID:9126 -> Cellular component: GO:0005634 [nucleus] evidence: TAS
GeneID:9126 -> Cellular component: GO:0005654 [nucleoplasm] evidence: TAS
GeneID:9126 -> Cellular component: GO:0005694 [chromosome] evidence: TAS
GeneID:9126 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
GeneID:9126 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
GeneID:9126 -> Cellular component: GO:0008278 [cohesin complex] evidence: NAS
GeneID:9126 -> Cellular component: GO:0016363 [nuclear matrix] evidence: IDA
GeneID:9126 -> Cellular component: GO:0030893 [meiotic cohesin complex] evidence: IDA
GeneID:9126 -> Cellular component: GO:0034991 [nuclear meiotic cohesin complex] evidence: IEA
by
@meso_cacase at
DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.